Search Results - "Zharikova, Anastasia"
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Expression of SARS-CoV-2 entry factors in lung epithelial stem cells and its potential implications for COVID-19
Published in Scientific reports (20-10-2020)“…SARS-CoV-2 can infiltrate the lower respiratory tract, resulting in severe respiratory failure and a high death rate. Normally, the airway and alveolar…”
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2
OrthoQuantum: visualizing evolutionary repertoire of eukaryotic proteins
Published in Nucleic acids research (05-07-2022)“…Abstract Extensive amounts of data from next-generation sequencing and omics studies have led to the accumulation of information that provides insight into the…”
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3
Gut Microbiota as a Source of Uremic Toxins
Published in International journal of molecular sciences (01-01-2022)“…Uremic retention solutes are the compounds that accumulate in the blood when kidney excretory function is impaired. Some of these compounds are toxic at high…”
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SARS‐CoV‐2 cellular tropism and direct multiorgan failure in COVID‐19 patients: Bioinformatic predictions, experimental observations, and open questions
Published in Cell biology international (01-02-2023)“…Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), the virus that causes coronavirus disease 2019 (COVID‐19), has led to an unprecedented public…”
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5
Do Extracellular Vesicles Derived from Mesenchymal Stem Cells Contain Functional Mitochondria?
Published in International journal of molecular sciences (03-07-2022)“…Extracellular vesicles (EV) derived from stem cells have become an effective complement to the use in cell therapy of stem cells themselves, which has led to…”
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Compensatory reactions of B cells in response to chronic HIV-1 Tat exposure
Published in Journal of cellular physiology (07-10-2024)“…Patients infected with human immunodeficiency virus-1 (HIV-1) have an increased incidence of B-cell lymphoma, even though HIV-1 does not infect B cells. The…”
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7
Intragenic compensation through the lens of deep mutational scanning
Published in Biophysical reviews (01-10-2022)“…A significant fraction of mutations in proteins are deleterious and result in adverse consequences for protein function, stability, or interaction with other…”
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Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot Study
Published in International journal of molecular sciences (01-09-2023)“…Familial dysbetalipoproteinemia (FD) is a highly atherogenic genetically based lipid disorder with an underestimated actual prevalence. In recent years,…”
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Analysis of the brain transcriptome, microbiome and metabolome in ketogenic diet and experimental stroke
Published in Brain, behavior, and immunity (01-01-2025)“…•KD affected brain gene expression, gut microbiome and blood metabolic profile.•Stroke induced alteration in brain transcriptome toward damage pattern.•Stroke…”
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Mesenchymal stromal cell-derived extracellular vesicles afford neuroprotection by modulating PI3K/AKT pathway and calcium oscillations
Published in International journal of biological sciences (01-01-2022)“…Mesenchymal stromal cells (MSC) are widely recognized as potential effectors in neuroprotective therapy. The protective properties of MSC were considered to be…”
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11
Differential Analysis of A-to-I mRNA Edited Sites in Parkinson's Disease
Published in Genes (22-12-2021)“…Parkinson's disease (PD) is a widespread neuronal degenerative disorder with unexplored etiology. It is associated with various pathological events. In…”
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BaRDIC: robust peak calling for RNA–DNA interaction data
Published in NAR genomics and bioinformatics (01-06-2024)“…Abstract Chromatin-associated non-coding RNAs play important roles in various cellular processes by targeting genomic loci. Two types of genome-wide NGS…”
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Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region
Published in Frontiers in genetics (07-10-2021)“…We performed a targeted sequencing of 242 clinically important genes mostly associated with cardiovascular diseases in a representative population sample of…”
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A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities
Published in International journal of molecular sciences (01-07-2024)“…A genetic diagnosis of primary cardiomyopathies can be a long-unmet need in patients with complex phenotypes. We investigated a three-generation family with…”
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Noncompaction cardiomyopathy is caused by a novel in‐frame desmin (DES) deletion mutation within the 1A coiled‐coil rod segment leading to a severe filament assembly defect
Published in Human mutation (01-06-2019)“…Mutations in DES, encoding desmin protein, are associated with different kinds of skeletal and/or cardiac myopathies. However, it is unknown, whether DES…”
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Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset
Published in International journal of molecular sciences (06-04-2021)“…About 50% of patients with arrhythmogenic cardiomyopathy (ACM) carry a pathogenic or likely pathogenic mutation in the desmosomal genes. However, there is a…”
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The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report
Published in International journal of molecular sciences (01-07-2021)“…Left ventricular non-compaction cardiomyopathy (LVNC) is a rare heart disease, with or without left ventricular dysfunction, which is characterized by a…”
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Ectopic expression of HIV-1 Tat modifies gene expression in cultured B cells: implications for the development of B-cell lymphomas in HIV-1-infected patients
Published in PeerJ (San Francisco, CA) (18-10-2022)“…An increased frequency of B-cell lymphomas is observed in human immunodeficiency virus-1 (HIV-1)-infected patients, although HIV-1 does not infect B cells…”
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FACS Isolation of Viable Cells in Different Cell Cycle Stages from Asynchronous Culture for RNA Sequencing
Published in Methods in molecular biology (Clifton, N.J.) (2018)“…Recently developed high-throughput analytical techniques (e.g., protein mass spectrometry and nucleic acid sequencing) allow unprecedentedly sensitive,…”
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Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases
Published in Journal of personalized medicine (12-07-2022)“…Cystic fibrosis, phenylketonuria, alpha-1 antitrypsin deficiency, and sensorineural hearing loss are among the most common autosomal recessive diseases, which…”
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